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Short-read sequencing for genomic profiling is useful for identifying disease-related variation in both DNA and RNA. However, molecular profiling utilising long-read sequencing enhances the resolution of such events because structural variation in cancer occurs often. For instance, the Pacific Biosciences long-read RNA-sequencing (Iso-Seq) transcri... Read More»
: Arch Sci 2022, 6: 139
10.4172/science.1000139Abstract Peer-reviewed Full Article Peer-reviewed Article PDF Mobile Full Article
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